Lu Qi, Wang Li, Gao Yabiao, Zhu Ping, Li Luying, Wang Xue, Jin Youping, Zhi Xiuling, Yu Jerry, Li Xin, Qin Xingjun, Zhou Ping
Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Fudan University, No. 130 Dong'an Road, Shanghai, 200032, China.
Institutes of Biomedical Sciences, Fudan University, No. 130 Dong'an Road, Shanghai, 200032, China.
Cancer Cell Int. 2021 Apr 26;21(1):232. doi: 10.1186/s12935-021-01916-w.
Anoikis resistance plays a critical role in the tumor metastasis by allowing survival of cancer cells in the systemic circulation. We previously showed that long non-coding RNAs APOC1P1-3 (lncRNA APOC1P1-3) inhibit apoptosis of breast cancer cells. In this study, we explored its role in anoikis resistance.
We induced anoikis resistance in two breast cancer cell lines (MCF-7 and MDA-MB-231) under anchorage-independent culture conditions and studied lncRNA APOC1P1-3 effects on apoptosis. Using Dual-Luciferase activity assay, we determined whether it specifically binds to miRNA-188-3P. We further explored its role in lung metastasis by injecting MDA-MB-231 and MDA-MB-231-APOC1P1-3-knock-down cells in female BALB/c nude mice.
We found that lncRNA APOC1P1-3 suppressed early apoptosis of these cells (demonstrated by gain or loss of their function, respectively) and promoted anoikis resistance via reducing activated- Caspase 3, 8, 9 and PARP. Moreover, it specifically binds to the target miRNA-188-3p acting as a "sponge" to block the inhibition of Bcl-2 (an anti-apoptosis protein).
Our study supports a theory that lncRNA APOC1P1-3 can promote development of breast cancer metastasis via anoikis resistance by specifically binding to miRNA-188-3p to block the inhibition of Bcl-2.
失巢凋亡抗性通过使癌细胞在体循环中存活,在肿瘤转移中起关键作用。我们之前表明长链非编码RNA APOC1P1-3(lncRNA APOC1P1-3)可抑制乳腺癌细胞凋亡。在本研究中,我们探讨了其在失巢凋亡抗性中的作用。
我们在无锚定培养条件下诱导两种乳腺癌细胞系(MCF-7和MDA-MB-231)产生失巢凋亡抗性,并研究lncRNA APOC1P1-3对细胞凋亡的影响。使用双荧光素酶活性测定法,我们确定它是否特异性结合miRNA-188-3P。我们通过将MDA-MB-231和MDA-MB-231-APOC1P1-3敲低细胞注射到雌性BALB/c裸鼠体内,进一步探讨其在肺转移中的作用。
我们发现lncRNA APOC1P1-3抑制这些细胞的早期凋亡(分别通过其功能获得或丧失来证明),并通过减少活化的半胱天冬酶3、8、9和PARP来促进失巢凋亡抗性。此外,它特异性结合靶标miRNA-188-3p,充当“海绵”以阻断对Bcl-2(一种抗凋亡蛋白)的抑制。
我们的研究支持一种理论,即lncRNA APOC1P1-3可通过特异性结合miRNA-188-3p以阻断对Bcl-2的抑制,通过失巢凋亡抗性促进乳腺癌转移的发展。